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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173935Generated: November 1, 2026

Tetrahydrofuran → (4-aminobenzyl)cyclohexylcarbamic Acid Benzyl Ester

https://huagongshe.com/reaction/1173935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactantcyclohexyl(4-nitrobenzyl)carbamic Acid Benzyl EsterHCID 66941326—
CatalystTrichloroiron;hexahydrateHCID 16211236—
SolventMethanolHCID 887—
Product(4-aminobenzyl)cyclohexylcarbamic Acid Benzyl EsterHCID 66941928101%

Reaction Steps

The compound (1.24 g) obtained in Example 87-1 was dissolved in methanol (12 ml) and THF (6.2 ml) and added with activated carbon (124 mg) and iron trichloride hexahydrate (12.4 mg), followed by thermal reflux for 0.5 hour. After standing to cool, the solution was added with hydrazine monohydrate (0.89 ml) and then subjected to thermal reflux for 3 hours. After completion of the reaction, the resultant was filtrated through Celite and the solvent was then distilled off. The residue was dissolved in chloroform and washed with water. The solution was dried with anhydrous magnesium sulfate. The solvent was distilled off, thereby obtaining the subject compound (1.15 g) as a yellow viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833991B2
Source datasetuspto-grants-2010_11
ORD IDord-50a3f51f8be7497e84fe7db6258d752c
Source noteuspto-grants-2010_11